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Recruiting Observational

Molecularly Redefining Small Bowel Adenocarcinoma to Accelerate Precision Patient Care

NCT06234306 · tracked via the Priya Life Science Denmark tracker
Phase
Observational
Started
2024-01-01
Last updated
2024-01-31

Condition(s) studied

Small Bowel Adenocarcinoma

Study summary

Small bowel adenocarcinoma is a rare malignancy, and there is limited knowledge about its optimal clinical management and molecular background. The SBAMOL study is an observational biomarker study that aims to identify prognostic and predictive biomarkers. This effort is intended to lay the groundwork for personalized medicine tailored to this specific patient group.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion criteria: Patients with histologically verified small bowel adenocarcinoma Patients older than 18 years Exclusion criteria: Insufficient material for molecular testing Patients registered in Vævsanvendelsesregistret\& Vævsanvendelsesregistret; refers to a central Danish registry where patients can opt out of allowing their biological material to be used for purposes other than their own disease management.

Primary outcome measure(s)

  • Molecular characterization of patients with SBA using high-throughput DNA-, mRNA- and T-cell receptor sequencing and targeted protein expression analyses. — 5 years
    Due to the scarce knowledge of the biological background of SBA. The primary endpoint of the study is to present a comprehensive descriptive molecular characterisation of patients with SBA.

Trial sites (3)

FacilityCityRegionStatus
Department of Oncology, Aarhus University Hospital Aarhus N Denmark Recruiting
Department Surgical Gastroenterology, Copenhagen University Hospital - Rigshospitalet Copenhagen Ø Denmark Recruiting
Department of Oncology Copenhagen University Hospital - Herlev and Gentofte Herlev Denmark Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06234306 on ClinicalTrials.gov ↗ ← All trials in Denmark